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LOX 抗体 (AA 22-168)

The 小鼠 单克隆 anti-LOX antibody is suitable to detect LOX in samples from 人. It has been validated for WB, IHC, FACS 和 IF.
产品编号 ABIN2725060
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for LOX 抗体 (AA 22-168) (ABIN2725060)

抗原

See all LOX 抗体
LOX (Lysyl Oxidase (LOX))

适用

  • 78
  • 36
  • 30
  • 7
  • 1

宿主

  • 79
  • 12
  • 2
小鼠

克隆类型

  • 60
  • 33
单克隆

标记

  • 35
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  • 12
  • 6
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  • 3
  • 3
  • 3
  • 3
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This LOX antibody is un-conjugated

应用范围

  • 64
  • 35
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  • 16
  • 5
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  • 2
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Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunofluorescence (IF)

克隆位点

9G2
  • 抗原表位

    • 8
    • 7
    • 5
    • 5
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    • 4
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    AA 22-168

    产品特性

    Homo sapiens lysyl oxidase (LOX), transcript variant 1

    纯化方法

    Purified from mouse ascites fluids by affinity chromatography

    免疫原

    Human recombinant protein fragment corresponding to amino acids 22-168 of human LOX (NP_002308) produced in HEK293T cell.

    亚型

    IgG1
  • 应用备注

    WB 1:500, IHC 1:150, IF 1:100, FLOW 1:100,

    说明

    The concentration of the product may vary between diferrent lots.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5-1.0 mg/mL

    缓冲液

    PBS ( pH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C
  • 抗原

    LOX (Lysyl Oxidase (LOX))

    别名

    LOX

    背景

    The protein encoded by this gene is an extracellular copper enzyme that initiates the crosslinking of collagens and elastin. The enzyme catalyzes oxidative deamination of the epsilon-amino group in certain lysine and hydroxylysine residues of collagens and lysine residues of elastin. In addition to crosslinking extracellular matrix proteins, the encoded protein may have a role in tumor suppression. Defects in this gene are a cause of autosomal recessive cutis laxa type I (CL type I). Two transcript variants encoding different isoforms have been found for this gene.

    分子量

    46.8 kDa

    基因ID

    4015

    NCBI登录号

    NM_002317

    HGNC

    4015

    途径

    SARS-CoV-2 Protein Interactome
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